venlafaxine
- Product NDC
- 50090-4587
- 11-digit product format
- 500904587
- Labeler code
- 50090
- Product ID
- 50090-4587_201fb335-1e9a-4bfa-bf54-9e5305b0b72c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090555
- Marketing category
- ANDA
- Marketing start
- 2010-04-07
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-4587-0 | venlafaxine | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 50090-4587-1 | venlafaxine | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4587 | VENLAFAXINE (VENLAFAXINE HYDROCHLORIDE) TABLET [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 2 package rows | 20191106_07e103e6-a524-4555-b9c7-12eba95d661b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4587-0 | 50090458700 | 30 TABLET in 1 BOTTLE (50090-4587-0) | 30 tablet | 2019-10-08 | 0000-00-00 | No | No | Current |
| 50090-4587-1 | 50090458701 | 90 TABLET in 1 BOTTLE (50090-4587-1) | 90 tablet | 2019-10-08 | 0000-00-00 | No | No | Current |